bnip2[All Fields] AND 1[has_clinical] - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3890753	copy number variation	1	nstd102	human	Benign	GRCh37 chr15: 59,848,471-60,004,707 , GRCh38.p12 chr15: 59,556,272-59,712,508	BNIP2, RNA5SP396, 3 more genes
nsv3923831	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 59,858,093-59,998,176 , GRCh38 chr15: 59,565,894-59,705,977 , NCBI36 chr15: 57,645,385-57,785,468	BNIP2, RNA5SP396, 3 more genes
nsv4675006	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 59,926,966-59,984,655 , GRCh38.p12 chr15: 59,634,767-59,692,456	BNIP2, GTF2A2, 1 more genes
nsv4456194	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 59,862,040-59,970,994 , GRCh38.p12 chr15: 59,569,841-59,678,795	BNIP2, RNA5SP396, 3 more genes
nsv3916249	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 21,173,967-100,338,915 , GRCh37.p13 chr15: 23,622,526-102,521,392 , GRCh38.p12 chr15: 23,377,379-101,981,189	BNIP2, H3P40, 1616 more genes
nsv3919468	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 26,996,912-100,338,915 , GRCh37.p13 chr15: 29,209,620-102,521,392 , GRCh38.p12 chr15: 28,917,417-101,981,189	BNIP2, RNU6-18P, 1442 more genes
nsv3899878	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 54,713,558-62,769,295 , GRCh38.p12 chr15: 54,421,360-62,477,096	BNIP2, RAB27A, 120 more genes
nsv3921425	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 55,647,440-61,098,667 , GRCh37 chr15: 57,860,148-63,311,614 , GRCh38 chr15: 57,567,950-63,019,415	BNIP2, MESTP2, 86 more genes
nsv3913143	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr15: 57,456,076-61,907,285 , GRCh37 chr15: 57,748,274-62,199,484 , NCBI36 chr15: 55,535,566-59,986,776	BNIP2, HMGB1P51, 73 more genes
nsv3890748	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 58,088,503-62,221,756 , GRCh38.p12 chr15: 57,796,305-61,929,557	BNIP2, RPL28P4, 66 more genes
nsv3900281	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 20,016,811-102,493,540 , GRCh38.p12 chr15: 19,811,558-101,953,337	BNIP2, MYZAP, 1750 more genes
nsv3913581	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 18,323,354-100,338,915 , GRCh37.p13 chr15: 20,063,340-102,521,392 , GRCh38.p12 chr15: 19,858,087-101,981,189	BNIP2, MIR4513, 1754 more genes
nsv3904086	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 20,071,673-102,461,162 , GRCh38.p12 chr15: 19,866,420-101,920,959	BNIP2, TMEM202, 1747 more genes
nsv3905138	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 20,733,395-102,511,616 , GRCh38.p12 chr15: 20,528,156-101,971,413	BNIP2, FES, 1738 more genes
nsv3892955	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr15: 22,770,422-102,429,112 , GRCh38.p12 chr15: 23,319,714-101,888,909	BNIP2, FAM81A, 1614 more genes
nsv3876912	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 31,115,047-102,354,857 , GRCh38.p12 chr15: 30,822,844-101,814,654	BNIP2, RNU6-953P, 1385 more genes
nsv3899559	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 41,745,084-102,354,798 , GRCh38.p12 chr15: 41,452,886-101,814,595	BNIP2, CILP, 1176 more genes
nsv6637384	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 48,589,845-63,543,438 , GRCh38.p12 chr15: 48,297,648-63,251,239	BNIP2, LINC03065, 228 more genes
nsv4456196	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 48,000,433-60,747,551 , GRCh38.p12 chr15: 47,708,236-60,455,352	BNIP2, MIR1266, 199 more genes
nsv3905308	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr15: 59,297,293-102,480,888 , GRCh38.p12 chr15: 59,005,094-101,940,685	BNIP2, ACAN, 861 more genes

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dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

Origin

Study Type

Subject Phenotype Status

Additional filters

Search results

Items: 1 to 20 of 28

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Number of Variants: 20

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